Kubtec DIGIVIEW 395— 510(k) K151221

Substantially Equivalent

Kub Technologies, Inc.

FDA 510(k) clearance K151221 for Kubtec DIGIVIEW 395, Substantially Equivalent on 2015-06-23. Applicant: Kub Technologies, Inc..

Clearance details

Applicant: Kub Technologies, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2015-05-07
Decision date: 2015-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, CT, US

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